Looking to grow your career in clinical data analytics and risk-based monitoring? A Central Monitoring Lead job at GSK offers an excellent opportunity to work at the forefront of Risk-Based Quality Management (RBQM) and centralized monitoring in clinical trials. This hybrid role is open in Bangalore (India) and Warsaw, ideal for professionals with experience in clinical data, analytics, and monitoring.
๐ Job Overview
- Role: Central Monitoring Lead
- Company: GSK
- Location: Bangalore (Hybrid)
- Experience: 1โ3 years in central monitoring
- Employment Type: Full-time
- Job ID: 437893
- Posted On: April 13, 2026
๐ Key Responsibilities
As a Central Monitoring Lead, you will drive RBQM implementation and ensure high-quality clinical trial delivery through centralized monitoring and data analytics:
- Lead Risk-Based Quality Management (RBQM) implementation across clinical studies
- Oversee centralized monitoring (CM) and data analytics (DA) execution
- Collaborate with cross-functional teams (Clinical Ops, Stats, Safety, Data Management)
- Identify critical-to-quality (CTQ) factors and mitigate study risks
- Interpret data trends, signals, and analytics outputs during trial execution
- Ensure monitoring plans, QTL reports, and risk mitigation strategies are aligned
- Manage vendor deliverables and performance
- Act as SME for RBQM and centralized monitoring
- Train and mentor team members on RBQM tools and processes
๐ Qualifications & Skills
To qualify for this Central Monitoring Lead job at GSK, candidates should have:
- 1โ3 years of experience in central monitoring or clinical data review
- Strong understanding of RBQM tools and data analytics
- Knowledge of ICH-GCP guidelines and clinical trial regulations
- End-to-end exposure to clinical development lifecycle
- Ability to interpret data visualizations and analytics insights
- Excellent communication and stakeholder management skills
- Fluency in English (written & spoken)
๐ผ Benefits & Work Culture
GSK offers a competitive and employee-friendly work environment:
- Hybrid work model (2โ3 days office)
- Flexible working hours
- Health insurance, life insurance, and retirement benefits
- Annual performance bonus
- Learning and development opportunities
- Global exposure in clinical research and drug development
- Collaborative and inclusive workplace
๐ Why This Role Matters
This Central Monitoring Lead role is critical in modern clinical trials where data-driven decision-making and risk-based monitoring improve study quality, reduce costs, and accelerate drug development timelines. It is a strategic role bridging clinical operations and data science.
๐ฉ How to Apply
